ET Quick Temporary Abutment

GUDID 00810019241222

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00810019241222
• NIH Device Record Key: 769ffd63-c953-46ec-ac82-59c50420efbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET Quick Temporary Abutment
• Version Model Number: ETQTA401MNT
• Company DUNS: 796083090
• Company Name: HIOSSEN, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810019241222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161689

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-23
• Device Publish Date: 2019-05-15

On-Brand Devices [ET Quick Temporary Abutment]

• 00810019241321: ETQTA555RNT
• 00810019241314: ETQTA555RHT
• 00810019241307: ETQTA455RNT
• 00810019241291: ETQTA455RHT
• 00810019241284: ETQTA455MNT
• 00810019241277: ETQTA455MHT
• 00810019241260: ETQTA451RNT
• 00810019241253: ETQTA451RHT
• 00810019241246: ETQTA405MNT
• 00810019241239: ETQTA405MHT
• 00810019241222: ETQTA401MNT
• 00810019241215: ETQTA401MHT